ClinVar Miner

List of variants in gene PALB2 reported as benign for not provided

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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.3114-51= rs249936 0.99999
NM_024675.4(PALB2):c.2996+264T>C rs420259 0.33075
NM_024675.4(PALB2):c.2586+58C>T rs249954 0.31139
NM_024675.4(PALB2):c.2835-299G>T rs12926135 0.29071
NM_024675.4(PALB2):c.3113+325A>G rs8061190 0.20097
NM_024675.4(PALB2):c.3113+204G>A rs8060124 0.18173
NM_024675.4(PALB2):c.3201+101A>G rs249935 0.13018
NM_024675.4(PALB2):c.1676A>G (p.Gln559Arg) rs152451 0.12980
NM_024675.4(PALB2):c.3113+1376C>G rs369444 0.07316
NM_024675.4(PALB2):c.211+320G>A rs377343 0.05288
NM_024675.4(PALB2):c.-47G>A rs8053188 0.04991
NM_024675.4(PALB2):c.211+274C>T rs13332044 0.04603
NM_024675.4(PALB2):c.49-165C>G rs7198601 0.04594
NM_024675.4(PALB2):c.3201+95C>T rs76918977 0.03415
NM_024675.4(PALB2):c.211+191A>T rs150117355 0.02674
NM_024675.4(PALB2):c.3300T>G (p.Thr1100=) rs45516100 0.02529
NM_024675.4(PALB2):c.2014G>C (p.Glu672Gln) rs45532440 0.02171
NM_024675.4(PALB2):c.629C>T (p.Pro210Leu) rs57605939 0.02101
NM_024675.4(PALB2):c.1684+29A>G rs74320059 0.01884
NM_024675.4(PALB2):c.2993G>A (p.Gly998Glu) rs45551636 0.01717
NM_024675.4(PALB2):c.1010T>C (p.Leu337Ser) rs45494092 0.01508
NM_024675.4(PALB2):c.925A>G (p.Ile309Val) rs3809683 0.00919
NM_024675.4(PALB2):c.2996+183del rs199767268 0.00748
NM_024675.4(PALB2):c.53A>G (p.Lys18Arg) rs138789658 0.00530
NM_024675.4(PALB2):c.2794G>A (p.Val932Met) rs45624036 0.00449
NM_024675.4(PALB2):c.1572A>G (p.Ser524=) rs45472400 0.00312
NM_024675.4(PALB2):c.1419A>C (p.Pro473=) rs62625275 0.00309
NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser) rs45568339 0.00287
NM_024675.4(PALB2):c.1810C>T (p.Leu604=) rs144015319 0.00202
NM_024675.4(PALB2):c.721A>G (p.Asn241Asp) rs113217267 0.00202
NM_024675.4(PALB2):c.1606C>T (p.Leu536=) rs151162255 0.00193
NM_024675.4(PALB2):c.2256A>G (p.Gly752=) rs147120218 0.00193
NM_024675.4(PALB2):c.400G>A (p.Asp134Asn) rs139555085 0.00160
NM_024675.4(PALB2):c.2742C>T (p.Phe914=) rs115759702 0.00143
NM_024675.4(PALB2):c.2816T>G (p.Leu939Trp) rs45478192 0.00121
NM_024675.4(PALB2):c.3495G>A (p.Ser1165=) rs45439097 0.00121
NM_024675.4(PALB2):c.1194G>A (p.Val398=) rs61755173 0.00103
NM_024675.4(PALB2):c.909C>T (p.Leu303=) rs145788619 0.00101
NM_024675.4(PALB2):c.2365C>T (p.Leu789=) rs145805054 0.00099
NM_024675.4(PALB2):c.23C>T (p.Pro8Leu) rs150390726 0.00051
NM_024675.4(PALB2):c.1470C>T (p.Pro490=) rs45612837 0.00035
NM_024675.4(PALB2):c.2834+15A>G rs149791114 0.00034
NM_024675.4(PALB2):c.1250C>A (p.Ser417Tyr) rs45510998 0.00011
NM_024675.4(PALB2):c.2027T>C (p.Ile676Thr) rs200875161 0.00011
NM_024675.4(PALB2):c.1623G>A (p.Arg541=) rs745665968 0.00009
NM_024675.4(PALB2):c.-10C>T rs1038099508 0.00006
NM_024675.4(PALB2):c.768C>T (p.Ser256=) rs45487491 0.00006
NM_024675.4(PALB2):c.2082A>G (p.Thr694=) rs781440401 0.00004
NM_024675.4(PALB2):c.3252G>A (p.Ser1084=) rs141570833 0.00004
NM_024675.4(PALB2):c.2748+15C>T rs749756493 0.00003
NM_024675.4(PALB2):c.109-5T>C rs749299119 0.00001
NM_024675.4(PALB2):c.1311A>G (p.Lys437=) rs190489275 0.00001
NM_024675.4(PALB2):c.2508C>G (p.Val836=) rs786203603 0.00001
NM_024675.4(PALB2):c.-48A>G rs1271474783
NM_024675.4(PALB2):c.15C>T (p.Pro5=) rs876658438
NM_024675.4(PALB2):c.1684+183TAAA[11] rs60066032
NM_024675.4(PALB2):c.1684+183TAAA[12] rs60066032
NM_024675.4(PALB2):c.1684+183TAAA[7] rs60066032
NM_024675.4(PALB2):c.1684+183TAAA[9] rs60066032
NM_024675.4(PALB2):c.1881G>T (p.Val627=) rs139362268
NM_024675.4(PALB2):c.212-24TA[4] rs751741705
NM_024675.4(PALB2):c.2586+15C>A rs144625889
NM_024675.4(PALB2):c.2607C>T (p.Ser869=) rs45542234
NM_024675.4(PALB2):c.2748+306C>G rs703776
NM_024675.4(PALB2):c.2835-71del rs754470879
NM_024675.4(PALB2):c.2835-72_2835-71del rs754470879
NM_024675.4(PALB2):c.3210C>G (p.Leu1070=) rs876659540
NM_024675.4(PALB2):c.3351-53del rs35294437

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